rs1057518093

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057518093(A;A)

Make rs1057518093(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

152139792

Gene

KMT2C

is a	snp
is	mentioned by
dbSNP	rs1057518093
dbSNP (classic)	rs1057518093
ClinGen	rs1057518093
ebi	rs1057518093
HLI	rs1057518093
Exac	rs1057518093
Gnomad	rs1057518093
Varsome	rs1057518093
LitVar	rs1057518093
Map	rs1057518093
PheGenI	rs1057518093
Biobank	rs1057518093
1000 genomes	rs1057518093
hgdp	rs1057518093
ensembl	rs1057518093
geneview	rs1057518093
scholar	rs1057518093
google	rs1057518093
pharmgkb	rs1057518093
gwascentral	rs1057518093
openSNP	rs1057518093
23andMe	rs1057518093
SNPshot	rs1057518093
SNPdbe	rs1057518093
MSV3d	rs1057518093
GWAS Ctlg	rs1057518093

Max Magnitude

0

ClinVar
Risk	rs1057518093(A;A)
Alt	rs1057518093(A;A)
Reference	Rs1057518093(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KMT2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.151836877C>T
CLNSRC
CLNACC	RCV000414032.1,